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combisan

EUDAMED

Class IIa (EU MDR)

Ref 80500.10Model combisan

by LED SpA

Identity

Trade Name
combisan EUDAMED
Device Name
combisan EUDAMED
Model / Reference
combisan EUDAMED
80500.10 EUDAMED

Identifiers

Primary DI / UDI-DI
08033638324219 EUDAMED
Basic UDI-DI
803363832STE002AD EUDAMED
Direct Marketing DI
08033638324219 EUDAMED
EMDN Code
Z120606,Z120615,Z12069080 EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

combisan by Led Spa — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
LED SpA
EUDAMED SRN
IT-MF-000012232

Sources (1)

  • EUDAMED c1472c19-d3cc-4773-8a45-6397de68e950 61 fields · synced Jun 19, 2026